MYO-MRI diagnostic protocols in genetic myopathies
•Whole body MRI (WBMRI) is an important imaging biomarker for myopathies.•Different mutations within the same gene can have different clinical WBMRI patterns.•WBMRI assesses all muscles in face, limbs and trunk not imaged in standard protocols.•MRI sequences measure atrophy / fatty infiltration (T1)...
Saved in:
Published in | Neuromuscular disorders : NMD Vol. 29; no. 11; pp. 827 - 841 |
---|---|
Main Authors | , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier B.V
01.11.2019
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 0960-8966 1873-2364 1873-2364 |
DOI | 10.1016/j.nmd.2019.08.011 |
Cover
Abstract | •Whole body MRI (WBMRI) is an important imaging biomarker for myopathies.•Different mutations within the same gene can have different clinical WBMRI patterns.•WBMRI assesses all muscles in face, limbs and trunk not imaged in standard protocols.•MRI sequences measure atrophy / fatty infiltration (T1) and edema (T2 or STIR, IDEAL T2).•3-point Dixon sequences provide better quantification of muscle water and fat content.
Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and characterizing the progression of myopathies and muscular dystrophies. Whole-body MRI indications and diagnostic efficacy are becoming better defined with the increasing number of cases, publications and discussions within multidisciplinary working groups. Advanced Whole-body MRI protocols are rapid, lower cost, and well-tolerated by patients. Accurate interpretation of muscle Whole-body MRI requires a detailed knowledge of muscle anatomy and differential pattern of involvement in muscle diseases. With the surge in recently identified novel genetic myopathies, Whole-body MRI will become increasingly useful for phenotypic validation of genetic variants of unknown significance. In addition, Whole-body MRI will be progressively used as a biomarker for disease progression and quantify response to therapy with the emergence of novel disease modifying treatments. This review outlines Whole-body MRI indications and updates refined protocols and provides a comprehensive overview of the diagnostic utility and suggested methodology of Whole-body MRI for pediatric and adult patients with muscle diseases. |
---|---|
AbstractList | Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and characterizing the progression of myopathies and muscular dystrophies. Whole-body MRI indications and diagnostic efficacy are becoming better defined with the increasing number of cases, publications and discussions within multidisciplinary working groups. Advanced Whole-body MRI protocols are rapid, lower cost, and well-tolerated by patients. Accurate interpretation of muscle Whole-body MRI requires a detailed knowledge of muscle anatomy and differential pattern of involvement in muscle diseases. With the surge in recently identified novel genetic myopathies, Whole-body MRI will become increasingly useful for phenotypic validation of genetic variants of unknown significance. In addition, Whole-body MRI will be progressively used as a biomarker for disease progression and quantify response to therapy with the emergence of novel disease modifying treatments. This review outlines Whole-body MRI indications and updates refined protocols and provides a comprehensive overview of the diagnostic utility and suggested methodology of Whole-body MRI for pediatric and adult patients with muscle diseases. Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and characterizing the progression of myopathies and muscular dystrophies. Whole-body MRI indications and diagnostic efficacy are becoming better defined with the increasing number of cases, publications and discussions within multidisciplinary working groups. Advanced Whole-body MRI protocols are rapid, lower cost, and well-tolerated by patients. Accurate interpretation of muscle Whole-body MRI requires a detailed knowledge of muscle anatomy and differential pattern of involvement in muscle diseases. With the surge in recently identified novel genetic myopathies, Whole-body MRI will become increasingly useful for phenotypic validation of genetic variants of unknown significance. In addition, Whole-body MRI will be progressively used as a biomarker for disease progression and quantify response to therapy with the emergence of novel disease modifying treatments. This review outlines Whole-body MRI indications and updates refined protocols and provides a comprehensive overview of the diagnostic utility and suggested methodology of Whole-body MRI for pediatric and adult patients with muscle diseases.Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and characterizing the progression of myopathies and muscular dystrophies. Whole-body MRI indications and diagnostic efficacy are becoming better defined with the increasing number of cases, publications and discussions within multidisciplinary working groups. Advanced Whole-body MRI protocols are rapid, lower cost, and well-tolerated by patients. Accurate interpretation of muscle Whole-body MRI requires a detailed knowledge of muscle anatomy and differential pattern of involvement in muscle diseases. With the surge in recently identified novel genetic myopathies, Whole-body MRI will become increasingly useful for phenotypic validation of genetic variants of unknown significance. In addition, Whole-body MRI will be progressively used as a biomarker for disease progression and quantify response to therapy with the emergence of novel disease modifying treatments. This review outlines Whole-body MRI indications and updates refined protocols and provides a comprehensive overview of the diagnostic utility and suggested methodology of Whole-body MRI for pediatric and adult patients with muscle diseases. •Whole body MRI (WBMRI) is an important imaging biomarker for myopathies.•Different mutations within the same gene can have different clinical WBMRI patterns.•WBMRI assesses all muscles in face, limbs and trunk not imaged in standard protocols.•MRI sequences measure atrophy / fatty infiltration (T1) and edema (T2 or STIR, IDEAL T2).•3-point Dixon sequences provide better quantification of muscle water and fat content. Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and characterizing the progression of myopathies and muscular dystrophies. Whole-body MRI indications and diagnostic efficacy are becoming better defined with the increasing number of cases, publications and discussions within multidisciplinary working groups. Advanced Whole-body MRI protocols are rapid, lower cost, and well-tolerated by patients. Accurate interpretation of muscle Whole-body MRI requires a detailed knowledge of muscle anatomy and differential pattern of involvement in muscle diseases. With the surge in recently identified novel genetic myopathies, Whole-body MRI will become increasingly useful for phenotypic validation of genetic variants of unknown significance. In addition, Whole-body MRI will be progressively used as a biomarker for disease progression and quantify response to therapy with the emergence of novel disease modifying treatments. This review outlines Whole-body MRI indications and updates refined protocols and provides a comprehensive overview of the diagnostic utility and suggested methodology of Whole-body MRI for pediatric and adult patients with muscle diseases. |
Author | Udd, Bjarne Carlier, Robert Y Bönnemann, Carsten G. Vissing, John Yousry, Tarek Hanna, Michael Warman Chardon, Jodi Muntoni, Francesco Straub, Volker Tasca, Giorgio Mercuri, Eugenio Gómez-Andrés, David Díaz-Manera, Jordi Fernández-Torrón, Roberto Heerschap, Arend Pichiecchio, Anna Walter, Maggie C. Quijano-Roy, Susana Ricci, Enzo Jungbluth, Heinz Morrow, Jasper M. |
Author_xml | – sequence: 1 givenname: Jodi surname: Warman Chardon fullname: Warman Chardon, Jodi organization: Neuromuscular Centre. The Ottawa Hospital, Canada – sequence: 2 givenname: Jordi surname: Díaz-Manera fullname: Díaz-Manera, Jordi organization: Neuromuscular Disorders Unit, Neurology department, Hospital Universitari de la Santa Creu i Sant Pau, Spain – sequence: 3 givenname: Giorgio surname: Tasca fullname: Tasca, Giorgio organization: Neurology, Fondazione Policlinico A. Gemelli IRCSS, Italy – sequence: 4 givenname: Carsten G. surname: Bönnemann fullname: Bönnemann, Carsten G. organization: National Institute of Neurological Disorders and Stroke, National Institute of Health, United States – sequence: 5 givenname: David surname: Gómez-Andrés fullname: Gómez-Andrés, David organization: Pediatric Neurology, Hospital Universitari Vall d'Hebron, Spain – sequence: 6 givenname: Arend surname: Heerschap fullname: Heerschap, Arend organization: Department of Radiology, Radboud University Nijmegen Medical Center, the Netherlands – sequence: 7 givenname: Eugenio surname: Mercuri fullname: Mercuri, Eugenio organization: Pediatric Neurology, Catholic University, Policlinico Gemelli, Italy – sequence: 8 givenname: Francesco surname: Muntoni fullname: Muntoni, Francesco organization: Paediatric Neurology, Dubowitz Neuromuscular Centre, UCL Institute of Child Health and Great Ormond Street Hospital for Children, UK – sequence: 9 givenname: Anna surname: Pichiecchio fullname: Pichiecchio, Anna organization: University of Pavia and Department of Neuroradiology IRCCS Mondino Foundation Pavia, Italy – sequence: 10 givenname: Enzo surname: Ricci fullname: Ricci, Enzo organization: Institute of Neurology, Catholic University, Italy – sequence: 11 givenname: Maggie C. surname: Walter fullname: Walter, Maggie C. organization: Friedrich-Baur Institut, Dept. of Neurology, Ludwig-Maximilians University Munich, Germany – sequence: 12 givenname: Michael surname: Hanna fullname: Hanna, Michael organization: Department of Neuromuscular Diseases, University College London, Queen Square Institute of Neurology, UK – sequence: 13 givenname: Heinz surname: Jungbluth fullname: Jungbluth, Heinz organization: Paediatric Neurology, King's College London, UK – sequence: 14 givenname: Jasper M. surname: Morrow fullname: Morrow, Jasper M. organization: Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, UK – sequence: 15 givenname: Roberto surname: Fernández-Torrón fullname: Fernández-Torrón, Roberto organization: Biodonostia Health Research Institute, Neuromuscular Area, Hospital Donostia, Neurology Department, 20014 Donostia - San Sebastian, Spain – sequence: 16 givenname: Bjarne surname: Udd fullname: Udd, Bjarne organization: Neuromuscular Centre, University of Tampere, Finland – sequence: 17 givenname: John surname: Vissing fullname: Vissing, John organization: Copenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Denmark – sequence: 18 givenname: Tarek surname: Yousry fullname: Yousry, Tarek organization: Neuroradiology, University College London, UK – sequence: 19 givenname: Susana surname: Quijano-Roy fullname: Quijano-Roy, Susana organization: APHP, Neuromuscular Unit, Department of Pediatric Neurology and Intensive cares, CHU Raymond Poincare (UVSQ), Garches, France – sequence: 20 givenname: Volker surname: Straub fullname: Straub, Volker organization: John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, UK – sequence: 21 givenname: Robert Y surname: Carlier fullname: Carlier, Robert Y email: robert.carlier@aphp.fr organization: Robert-Yves Carlier, Service de Radiologie et Imagerie Médicale Hôpital Raymond Poincaré, Hôpitaux de Paris (AP-HP), Garches, France |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31727541$$D View this record in MEDLINE/PubMed https://hal.science/hal-03488911$$DView record in HAL |
BookMark | eNqFkEFLHDEYhoNYdLX9Ab2UPdbDTL8vmUky9CRiq7AilPbQU8gkWc12JtlOssL-e7OsevCgp8DH87yE54QchhgcIZ8RagTk31Z1GG1NAbsaZA2IB2SGUrCKMt4ckhl0HCrZcX5MTlJaAWAruDgixwwFFW2DM0Jv_t5WN7-u59bruxBT9ma-nmKOJg5p7sP8zgW3O47buNb53rv0kXxY6iG5T0_vKfnz4_L3xVW1uP15fXG-qEzDRK5a6JmxXdu1ljPdsaa3ErDpBfS8XXKJKGyL0jjJtAbJW0lNiyBo30sLS8FOydl-914Paj35UU9bFbVXV-cLtbsBa6TsEB-wsF_3bPn7_41LWY0-GTcMOri4SYoyLNu0oVDQL0_oph-dfVl-blIAsQfMFFOa3FIZn3X2MeRJ-0EhqF19tVKlvtrVVyBVqV9MfGU-j7_lfN87rqR88G5SyXgXjLN-ciYrG_2bdvfKNoMP3ujhn9u-4z4CFZysNQ |
CitedBy_id | crossref_primary_10_1016_j_diii_2022_01_012 crossref_primary_10_1016_j_neurol_2022_11_007 crossref_primary_10_1007_s00415_020_09862_9 crossref_primary_10_1007_s00415_023_11862_4 crossref_primary_10_3233_JND_200543 crossref_primary_10_1016_j_inffus_2020_07_006 crossref_primary_10_1016_j_nmd_2021_07_397 crossref_primary_10_1002_acn3_51760 crossref_primary_10_1177_22143602241289705 crossref_primary_10_1186_s12014_023_09412_1 crossref_primary_10_1007_s00115_024_01673_x crossref_primary_10_1016_j_nmd_2023_08_011 crossref_primary_10_1016_j_jep_2021_114359 crossref_primary_10_1016_j_neurol_2022_12_002 crossref_primary_10_1055_a_1738_5356 crossref_primary_10_1016_j_nmd_2022_10_005 crossref_primary_10_1016_j_nmd_2022_09_010 crossref_primary_10_1055_s_0040_1712955 crossref_primary_10_1007_s00117_024_01276_2 crossref_primary_10_1007_s00415_021_10786_1 crossref_primary_10_1080_14728222_2022_2157258 crossref_primary_10_1002_jcsm_13089 crossref_primary_10_1007_s00415_020_09872_7 crossref_primary_10_1080_14789450_2020_1773806 crossref_primary_10_3389_fneur_2023_1251025 crossref_primary_10_1016_j_nmd_2023_09_010 crossref_primary_10_1093_rheumatology_keae505 crossref_primary_10_3390_brainsci13101500 crossref_primary_10_3390_genes12111786 crossref_primary_10_3389_fneur_2020_613446 crossref_primary_10_1007_s00112_021_01319_1 crossref_primary_10_1007_s00415_021_10806_0 crossref_primary_10_1038_s41419_022_05233_6 crossref_primary_10_1111_ene_14630 crossref_primary_10_3390_ijms252312994 crossref_primary_10_1007_s00415_024_12544_5 crossref_primary_10_1016_j_cppeds_2021_101033 crossref_primary_10_1111_ene_15174 crossref_primary_10_1002_mus_27638 crossref_primary_10_1186_s42047_024_00165_1 crossref_primary_10_1097_WCO_0000000000000851 crossref_primary_10_1016_j_ejrad_2024_111481 crossref_primary_10_1055_s_0040_1713714 crossref_primary_10_1097_BOR_0000000000001043 crossref_primary_10_1097_WCO_0000000000001305 crossref_primary_10_1002_mus_27099 crossref_primary_10_1016_j_nmd_2021_08_006 crossref_primary_10_3233_JND_219001 |
Cites_doi | 10.1007/s00247-016-3777-6 10.1017/cjn.2018.314 10.1002/jmri.21492 10.1001/jamaneurol.2015.2274 10.1053/ejpn.2002.0618 10.1002/mus.26403 10.1007/s00415-017-8547-3 10.1007/s00330-008-1071-1 10.1016/j.nmd.2016.10.006 10.1016/j.diii.2013.05.008 10.2214/AJR.17.17849 10.1016/S0960-8966(03)00091-9 10.1016/j.nmd.2015.10.001 10.1016/j.spen.2011.10.003 10.1007/s00415-016-8361-3 10.1007/s00330-018-5472-5 10.1016/S0960-8966(02)00023-8 10.1016/S1474-4422(15)00242-2 10.1016/j.nmd.2011.06.748 10.1016/j.nmd.2012.08.002 10.1002/mus.24634 10.1016/j.nmd.2012.08.003 10.1016/j.nmd.2012.08.001 10.1259/0007-1285-62-736-326 10.1186/s13395-018-0163-0 10.1016/S0730-725X(98)00080-0 10.1016/j.nmd.2012.05.012 10.1148/radiology.153.1.6089263 10.1259/0007-1285-63-756-946 10.1097/BOR.0b013e3282efdc66 10.1016/j.nmd.2012.06.347 10.1016/j.bbrc.2012.10.127 10.1053/ejpn.2002.0617 10.1111/ene.12984 10.1007/s00330-010-1799-2 10.1007/s00415-018-9037-y 10.1002/acn3.319 10.1016/0720-048X(92)90113-N 10.3174/ajnr.A4596 10.1016/j.ncl.2004.03.008 10.1212/WNL.0b013e31826e9b73 10.1097/WCO.0000000000000364 10.4081/bam.2015.2.121 10.1016/j.nmd.2012.06.005 10.1002/mus.25045 10.1055/s-0034-1389894 10.1016/j.nmd.2005.01.004 10.3389/fneur.2018.00456 10.1002/mus.25608 10.1002/mus.24653 10.1016/j.nmd.2016.09.002 10.1002/ana.21846 10.3233/JND-160145 10.1097/01.wco.0000183947.01362.fe 10.1016/j.jocn.2016.01.041 10.1111/nan.12385 10.1016/j.nmd.2007.03.015 10.1007/s00330-004-2270-z 10.1371/journal.pone.0181069 10.3233/JND-180333 10.1002/mus.24609 10.1111/j.1600-0404.2008.01129.x 10.1007/s11926-015-0544-x 10.1007/s00256-014-1909-3 10.1007/s00415-019-09437-3 10.1002/jmri.20804 10.1002/mus.24569 10.1002/mus.25018 10.1093/hmg/dds514 10.1016/j.nmd.2015.10.003 |
ContentType | Journal Article |
Copyright | 2019 Elsevier B.V. Copyright © 2019 Elsevier B.V. All rights reserved. Attribution - NonCommercial |
Copyright_xml | – notice: 2019 Elsevier B.V. – notice: Copyright © 2019 Elsevier B.V. All rights reserved. – notice: Attribution - NonCommercial |
CorporateAuthor | MYO-MRI Working Group |
CorporateAuthor_xml | – name: MYO-MRI Working Group |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 1XC VOOES |
DOI | 10.1016/j.nmd.2019.08.011 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic Hyper Article en Ligne (HAL) Hyper Article en Ligne (HAL) (Open Access) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1873-2364 |
EndPage | 841 |
ExternalDocumentID | oai_HAL_hal_03488911v1 31727541 10_1016_j_nmd_2019_08_011 S0960896619311022 |
Genre | Research Support, Non-U.S. Gov't Journal Article Review |
GrantInformation_xml | – fundername: Medical Research Council grantid: MR/M009106/1 |
GroupedDBID | --- --K --M .1- .FO .GJ .~1 0R~ 123 1B1 1P~ 1RT 1~. 1~5 29N 4.4 457 4G. 53G 5VS 7-5 71M 8P~ 9JM AABNK AAEDT AAEDW AAIKJ AAKOC AALRI AAOAW AAQFI AAQXK AATTM AAXKI AAXLA AAXUO AAYWO ABBQC ABCQJ ABFNM ABFRF ABJNI ABLJU ABMAC ABMZM ABTEW ABWVN ABXDB ACDAQ ACGFO ACGFS ACIEU ACIUM ACRLP ACRPL ACVFH ADBBV ADCNI ADEZE ADMUD ADNMO ADVLN AEBSH AEFWE AEIPS AEKER AENEX AEUPX AEVXI AFJKZ AFPUW AFRHN AFTJW AFXIZ AGCQF AGHFR AGQPQ AGUBO AGWIK AGYEJ AHHHB AIEXJ AIGII AIIUN AIKHN AITUG AJRQY AJUYK AKBMS AKRLJ AKRWK AKYEP ALMA_UNASSIGNED_HOLDINGS AMRAJ ANKPU ANZVX APXCP ASPBG AVWKF AXJTR AZFZN BKOJK BLXMC BNPGV CS3 DU5 EBS EFJIC EFKBS EJD EO8 EO9 EP2 EP3 F5P FDB FEDTE FGOYB FIRID FNPLU FYGXN G-2 G-Q GBLVA HDW HMK HMO HMQ HVGLF HZ~ IHE J1W KOM LX8 M29 M2V M41 MO0 MOBAO N9A O-L O9- OAUVE OP~ OZT P-8 P-9 P2P PC. Q38 R2- ROL RPZ SAE SCC SDF SDG SDP SEL SES SEW SNS SPCBC SSH SSN SSZ T5K UHS UNMZH WUQ Z5R ~G- AACTN AADPK AAIAV ABLVK ABYKQ AFCTW AFKWA AJBFU AJOXV AMFUW EFLBG LCYCR RIG ZA5 AAYXX AGRNS CITATION CGR CUY CVF ECM EIF NPM 7X8 ACLOT ~HD 1XC VOOES |
ID | FETCH-LOGICAL-c437t-50b3cd9595d63a934bd8014b70b65f68117d518ce83aa086582c51072bb8d0f73 |
IEDL.DBID | AIKHN |
ISSN | 0960-8966 1873-2364 |
IngestDate | Fri Sep 12 12:19:38 EDT 2025 Sat Sep 27 22:23:13 EDT 2025 Mon Jul 21 05:43:19 EDT 2025 Tue Jul 01 01:07:20 EDT 2025 Thu Apr 24 23:07:45 EDT 2025 Fri Feb 23 02:49:04 EST 2024 Tue Aug 26 16:46:51 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 11 |
Keywords | Inherited myopathy Congenital myopathy Limb girdle muscular dystrophy Magnetic resonance imaging Whole-body MRI Inflammatory myopathy |
Language | English |
License | Copyright © 2019 Elsevier B.V. All rights reserved. Attribution - NonCommercial: http://creativecommons.org/licenses/by-nc |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c437t-50b3cd9595d63a934bd8014b70b65f68117d518ce83aa086582c51072bb8d0f73 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
ORCID | 0000-0003-0849-9144 0000-0002-9851-5365 0000-0002-9102-5232 |
OpenAccessLink | https://hal.science/hal-03488911 |
PMID | 31727541 |
PQID | 2315102420 |
PQPubID | 23479 |
PageCount | 15 |
ParticipantIDs | hal_primary_oai_HAL_hal_03488911v1 proquest_miscellaneous_2315102420 pubmed_primary_31727541 crossref_citationtrail_10_1016_j_nmd_2019_08_011 crossref_primary_10_1016_j_nmd_2019_08_011 elsevier_sciencedirect_doi_10_1016_j_nmd_2019_08_011 elsevier_clinicalkey_doi_10_1016_j_nmd_2019_08_011 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2019-11-01 |
PublicationDateYYYYMMDD | 2019-11-01 |
PublicationDate_xml | – month: 11 year: 2019 text: 2019-11-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | Neuromuscular disorders : NMD |
PublicationTitleAlternate | Neuromuscul Disord |
PublicationYear | 2019 |
Publisher | Elsevier B.V Elsevier |
Publisher_xml | – name: Elsevier B.V – name: Elsevier |
References | Guimaraes, Zanoteli, Link, de Camargo, Facchetti, Nardo (bib0040) 2017; 209 Jarraya, Quijano-Roy, Monnier, Behin, Avila-Smirnov, Romero (bib0016) 2012; 22 Diaz, Woudt, Suazo, Garrido, Caviedes, AM (bib0018) 2016; 54 Straub, Carlier, Mercuri (bib0002) 2012; 22 Mercuri, Pichiecchio, Counsell, Allsop, Cini, Jungbluth (bib0003) 2002; 6 Lamminen, Hekali, Tiula, Suramo, Korhola (bib0008) 1989; 62 Polavarapu, Manjunath, Preethish-Kumar, Sekar, Vengalil, Thomas (bib0066) 2016; 26 Diaz-Manera, Alejaldre, Gonzalez, Olive, Gomez-Andres, Muelas (bib0039) 2016; 26 Dixon (bib0049) 1984; 153 Larson, Baker, Milev, Press, Sokol, Cox (bib0056) 2018; 8 Fiorillo, Brisca, Cassandrini, Scapolan, Astrea, Valle (bib0062) 2013; 430 Kesper, Kornblum, Reimann, Lutterbey, Schroder, Wattjes (bib0071) 2009; 120 Schedel, Reimers, Nagele, Witt, Pongratz, Vogl (bib0006) 1992; 15 Carlier, Mercuri, Straub (bib0014) 2012; 22 Noury, Bohm, Peche, Guyant-Marechal, Bedat-Millet, Chiche (bib0055) 2017; 27 Strijkers, Araujo, Azzabou, Bendahan, Blamire, Burakiewicz (bib0075) 2019; 6 Ohana, Durand, Marty, Lazareth, Maisonobe, Mompoint (bib0054) 2014; 43 Morrow, Sinclair, Fischmann, Machado, Reilly, Yousry (bib0019) 2016; 15 Quijano-Roy, Carlier, Fischer (bib0032) 2011; 18 Ma (bib0050) 2008; 28 Hankiewicz, Carlier, Lazaro, Linzoain, Barnerias, Gomez-Andres (bib0072) 2015; 52 Mah, van Alfen (bib0023) 2018; 45 Elessawy, Abdelsalam, Abdel Razek, Tharwat (bib0046) 2016; 5 Ozsarlak, Parizel, De Schepper, De Jonghe, Martin (bib0038) 2004; 14 Lovitt, Marden, Gundogdu, Ostrowski (bib0011) 2004; 22 Mercuri, Clements, Offiah, Pichiecchio, Vasco, Bianco (bib0012) 2010; 67 Carlier, Laforet, Wary, Mompoint, Laloui, Pellegrini (bib0033) 2011; 21 Gomez-Andres, Dabaj, Mompoint, Hankiewicz, Azzi, Ioos (bib0017) 2016; 54 Mercuri, Jungbluth, Muntoni (bib0010) 2005; 18 Goutallier, Postel, Bernageau, Lavau, Voisin (bib0036) 1994 Schramm, Born, Weckbach, Reilich, Walter, Reiser (bib0070) 2008; 18 Leung (bib0034) 2016 Quijano-Roy, Carlier (bib0020) 2014; 45 Echaniz-Laguna, Carlier, Laloui, Carlier, Salort-Campana, Pouget (bib0061) 2015; 51 Mul, Horlings, Vincenten, Voermans, van Engelen, van Alfen (bib0059) 2018; 265 Ortolan, Zanato, Coran, Beltrame, Stramare (bib0028) 2015; 25 Papadopoulos, LaforEt, Nectoux, Stojkovic, Wahbi, Carlier (bib0053) 2017; 56 Crawford, Filli, Elliott, Nanz, Fischer, Marcon (bib0041) 2016; 37 Lamminen (bib0007) 1990; 63 Messineo, Cremona, Trinci, Francia, Marini (bib0009) 1998; 16 Gomez-Andres, Diaz, Munell, Sanchez-Montanez, Pulido-Valdeolivas, Suazo (bib0063) 2019; 59 Jungbluth (bib0027) 2017 Fischer, Bonati, Wattjes (bib0030) 2016; 29 Ghaoui, Cooper, Lek, Jones, Corbett, Reddel (bib0067) 2015; 72 Bugiardini, Morrow, Shah, Wood, Lynch, Pitmann (bib0013) 2018; 9 Burakiewicz, Sinclair, Fischer, Walter, Kan, Hollingsworth (bib0074) 2017; 264 Ten Dam, van der Kooi, Verhamme, Wattjes, de Visser (bib0015) 2016; 23 Simon, Noto, Zaidman (bib0025) 2016; 33 Mercuri, Lampe, Allsop, Knight, Pane, Kinali (bib0042) 2005; 15 Ohana, Moser, Moussaoui, Kremer, Carlier, Liverneaux (bib0045) 2014; 95 Andersen, Dahlqvist, Vissing, Heje, Thomsen, Vissing (bib0064) 2017; 264 Tordjman, Dabaj, Laforet, Felter, Ferreiro, Biyoukar (bib0058) 2018; 28 Brockmann, Becker, Schreiber, Neubert, Brunner, Bonnemann (bib0026) 2007; 17 Mercuri, Pichiecchio, Allsop, Messina, Pane, Muntoni (bib0037) 2007; 25 Cejas, Serra, Galvez, Cavassa, Taratuto, Vazquez (bib0021) 2017 ten Dam, van der Kooi, van Wattingen, de Haan, de Visser (bib0031) 2012; 79 Mercuri, Cini, Pichiecchio, Allsop, Counsell, Zolkipli (bib0043) 2003; 13 Evila, Arumilli, Udd, Hackman (bib0068) 2016; 26 Godi, Ambrosi, Nicastro, Previtali, Santarosa, Napolitano (bib0065) 2016; 3 Huang, Gao, Chen, Yang, Chen, Yan (bib0060) 2017; 12 Maurer, Walker (bib0048) 2015; 17 Mercuri, Cini, Counsell, Allsop, Zolkipli, Jungbluth (bib0004) 2002; 6 Carlier, Marty, Scheidegger, Loureiro de Sousa, Baudin, Snezhko (bib0073) 2016; 3 Leung, Carrino, Wagner, Jacobs (bib0022) 2015; 52 Sarkozy, Deschauer, Carlier, Schrank, Seeger, Walter (bib0035) 2012; 22 Reddy, Cho, Lek, Estrella, Valkanas, Jones (bib0069) 2016 Dieterich, Quijano-Roy, Monnier, Zhou, Faure, Smirnow (bib0044) 2013; 22 Wattjes, Kley, Fischer (bib0052) 2010; 20 Mercuri, Talim, Moghadaszadeh, Petit, Brockington, Counsell (bib0005) 2002; 12 Berardo, Lornage, Johari, Evangelista, Cejas, Barroso (bib0057) 2019 Diaz-Manera, Llauger, Gallardo, Illa (bib0024) 2015; 34 Quijano-Roy, Avila-Smirnow, Carlier (bib0001) 2012; 22 Kuo, Carrino (bib0047) 2007; 19 Zaidman, Malkus, Connolly (bib0029) 2015; 52 Hollingsworth, de Sousa, Straub, Carlier (bib0051) 2012; 22 Guimaraes (10.1016/j.nmd.2019.08.011_bib0040) 2017; 209 Carlier (10.1016/j.nmd.2019.08.011_bib0014) 2012; 22 Jungbluth (10.1016/j.nmd.2019.08.011_bib0027) 2017 Zaidman (10.1016/j.nmd.2019.08.011_bib0029) 2015; 52 Jarraya (10.1016/j.nmd.2019.08.011_bib0016) 2012; 22 Messineo (10.1016/j.nmd.2019.08.011_bib0009) 1998; 16 Strijkers (10.1016/j.nmd.2019.08.011_bib0075) 2019; 6 Mercuri (10.1016/j.nmd.2019.08.011_bib0004) 2002; 6 Maurer (10.1016/j.nmd.2019.08.011_bib0048) 2015; 17 Mercuri (10.1016/j.nmd.2019.08.011_bib0012) 2010; 67 Bugiardini (10.1016/j.nmd.2019.08.011_bib0013) 2018; 9 Wattjes (10.1016/j.nmd.2019.08.011_bib0052) 2010; 20 Straub (10.1016/j.nmd.2019.08.011_bib0002) 2012; 22 Reddy (10.1016/j.nmd.2019.08.011_bib0069) 2016 Carlier (10.1016/j.nmd.2019.08.011_bib0033) 2011; 21 Leung (10.1016/j.nmd.2019.08.011_bib0034) 2016 Sarkozy (10.1016/j.nmd.2019.08.011_bib0035) 2012; 22 Papadopoulos (10.1016/j.nmd.2019.08.011_bib0053) 2017; 56 Berardo (10.1016/j.nmd.2019.08.011_bib0057) 2019 Ohana (10.1016/j.nmd.2019.08.011_bib0054) 2014; 43 Brockmann (10.1016/j.nmd.2019.08.011_bib0026) 2007; 17 ten Dam (10.1016/j.nmd.2019.08.011_bib0031) 2012; 79 Ten Dam (10.1016/j.nmd.2019.08.011_bib0015) 2016; 23 Ohana (10.1016/j.nmd.2019.08.011_bib0045) 2014; 95 Ozsarlak (10.1016/j.nmd.2019.08.011_bib0038) 2004; 14 Gomez-Andres (10.1016/j.nmd.2019.08.011_bib0063) 2019; 59 Schedel (10.1016/j.nmd.2019.08.011_bib0006) 1992; 15 Andersen (10.1016/j.nmd.2019.08.011_bib0064) 2017; 264 Fischer (10.1016/j.nmd.2019.08.011_bib0030) 2016; 29 Quijano-Roy (10.1016/j.nmd.2019.08.011_bib0032) 2011; 18 Carlier (10.1016/j.nmd.2019.08.011_bib0073) 2016; 3 Fiorillo (10.1016/j.nmd.2019.08.011_bib0062) 2013; 430 Diaz-Manera (10.1016/j.nmd.2019.08.011_bib0039) 2016; 26 Dieterich (10.1016/j.nmd.2019.08.011_bib0044) 2013; 22 Hankiewicz (10.1016/j.nmd.2019.08.011_bib0072) 2015; 52 Gomez-Andres (10.1016/j.nmd.2019.08.011_bib0017) 2016; 54 Evila (10.1016/j.nmd.2019.08.011_bib0068) 2016; 26 Lamminen (10.1016/j.nmd.2019.08.011_bib0008) 1989; 62 Ma (10.1016/j.nmd.2019.08.011_bib0050) 2008; 28 Diaz (10.1016/j.nmd.2019.08.011_bib0018) 2016; 54 Mul (10.1016/j.nmd.2019.08.011_bib0059) 2018; 265 Simon (10.1016/j.nmd.2019.08.011_bib0025) 2016; 33 Godi (10.1016/j.nmd.2019.08.011_bib0065) 2016; 3 Hollingsworth (10.1016/j.nmd.2019.08.011_bib0051) 2012; 22 Elessawy (10.1016/j.nmd.2019.08.011_bib0046) 2016; 5 Lamminen (10.1016/j.nmd.2019.08.011_bib0007) 1990; 63 Cejas (10.1016/j.nmd.2019.08.011_bib0021) 2017 Kuo (10.1016/j.nmd.2019.08.011_bib0047) 2007; 19 Morrow (10.1016/j.nmd.2019.08.011_bib0019) 2016; 15 Mah (10.1016/j.nmd.2019.08.011_bib0023) 2018; 45 Leung (10.1016/j.nmd.2019.08.011_bib0022) 2015; 52 Ortolan (10.1016/j.nmd.2019.08.011_bib0028) 2015; 25 Quijano-Roy (10.1016/j.nmd.2019.08.011_bib0020) 2014; 45 Burakiewicz (10.1016/j.nmd.2019.08.011_bib0074) 2017; 264 Tordjman (10.1016/j.nmd.2019.08.011_bib0058) 2018; 28 Larson (10.1016/j.nmd.2019.08.011_bib0056) 2018; 8 Polavarapu (10.1016/j.nmd.2019.08.011_bib0066) 2016; 26 Crawford (10.1016/j.nmd.2019.08.011_bib0041) 2016; 37 Mercuri (10.1016/j.nmd.2019.08.011_bib0037) 2007; 25 Echaniz-Laguna (10.1016/j.nmd.2019.08.011_bib0061) 2015; 51 Ghaoui (10.1016/j.nmd.2019.08.011_bib0067) 2015; 72 Goutallier (10.1016/j.nmd.2019.08.011_bib0036) 1994 Kesper (10.1016/j.nmd.2019.08.011_bib0071) 2009; 120 Mercuri (10.1016/j.nmd.2019.08.011_bib0003) 2002; 6 Mercuri (10.1016/j.nmd.2019.08.011_bib0043) 2003; 13 Lovitt (10.1016/j.nmd.2019.08.011_bib0011) 2004; 22 Schramm (10.1016/j.nmd.2019.08.011_bib0070) 2008; 18 Mercuri (10.1016/j.nmd.2019.08.011_bib0010) 2005; 18 Dixon (10.1016/j.nmd.2019.08.011_bib0049) 1984; 153 Huang (10.1016/j.nmd.2019.08.011_bib0060) 2017; 12 Quijano-Roy (10.1016/j.nmd.2019.08.011_bib0001) 2012; 22 Noury (10.1016/j.nmd.2019.08.011_bib0055) 2017; 27 Diaz-Manera (10.1016/j.nmd.2019.08.011_bib0024) 2015; 34 Mercuri (10.1016/j.nmd.2019.08.011_bib0005) 2002; 12 Mercuri (10.1016/j.nmd.2019.08.011_bib0042) 2005; 15 |
References_xml | – volume: 33 start-page: 1 year: 2016 end-page: 10 ident: bib0025 article-title: Skeletal muscle imaging in neuromuscular disease publication-title: J Clin Neurosci – volume: 12 year: 2017 ident: bib0060 article-title: An efficacy analysis of whole-body magnetic resonance imaging in the diagnosis and follow-up of polymyositis and dermatomyositis publication-title: PLoS One – volume: 29 start-page: 614 year: 2016 end-page: 620 ident: bib0030 article-title: Recent developments in muscle imaging of neuromuscular disorders publication-title: Curr Opin Neurol – start-page: 78 year: 1994 end-page: 83 ident: bib0036 article-title: Fatty muscle degeneration in cuff ruptures. Pre- and postoperative evaluation by CT scan publication-title: Clin Orthop Relat Res. – volume: 26 start-page: 33 year: 2016 end-page: 40 ident: bib0039 article-title: Muscle imaging in muscle dystrophies produced by mutations in the emd and lmna genes publication-title: Neuromuscul Disord – volume: 21 start-page: 791 year: 2011 end-page: 799 ident: bib0033 article-title: Whole-body muscle mri in 20 patients suffering from late onset pompe disease: Involvement patterns publication-title: Neuromuscul Disord – volume: 12 start-page: 631 year: 2002 end-page: 638 ident: bib0005 article-title: Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1) publication-title: Neuromuscul Disord – volume: 14 start-page: 1489 year: 2004 end-page: 1493 ident: bib0038 article-title: Whole-body mr screening of muscles in the evaluation of neuromuscular diseases publication-title: Eur Radiol – volume: 15 start-page: 230 year: 1992 end-page: 238 ident: bib0006 article-title: Imaging techniques in myotonic dystrophy. a comparative study of ultrasound, computed tomography and magnetic resonance imaging of skeletal muscles publication-title: Eur J Radiol – volume: 6 start-page: 309 year: 2002 end-page: 314 ident: bib0004 article-title: Muscle mri findings in a three-generation family affected by bethlem myopathy publication-title: Eur J Paediatr Neurol – year: 2017 ident: bib0021 article-title: Muscle mri in pediatrics: clinical, pathological and genetic correlation publication-title: Pediatr Radiol – volume: 209 start-page: 1340 year: 2017 end-page: 1347 ident: bib0040 article-title: Sporadic inclusion body myositis: mri findings and correlation with clinical and functional parameters publication-title: AJR Am J Roentgenol – volume: 67 start-page: 201 year: 2010 end-page: 208 ident: bib0012 article-title: Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine publication-title: Ann Neurol – volume: 18 start-page: 2922 year: 2008 end-page: 2936 ident: bib0070 article-title: Involvement patterns in myotilinopathy and desminopathy detected by a novel neuromuscular whole-body mri protocol publication-title: Eur Radiol – volume: 62 start-page: 326 year: 1989 end-page: 330 ident: bib0008 article-title: Acute rhabdomyolysis: evaluation with magnetic resonance imaging compared with computed tomography and ultrasonography publication-title: Br J Radiol – volume: 20 start-page: 2447 year: 2010 end-page: 2460 ident: bib0052 article-title: Neuromuscular imaging in inherited muscle diseases publication-title: Eur Radiol – volume: 28 start-page: 543 year: 2008 end-page: 558 ident: bib0050 article-title: Dixon techniques for water and fat imaging publication-title: J Magn Reson Imaging – volume: 28 start-page: 5293 year: 2018 end-page: 5303 ident: bib0058 article-title: Muscular MRI-based algorithm to differentiate inherited myopathies presenting with spinal rigidity publication-title: Eur Radiol – volume: 22 start-page: S68 year: 2012 end-page: S84 ident: bib0001 article-title: Whole body muscle mri protocol: pattern recognition in early onset nm disorders publication-title: Neuromuscul Disord – volume: 59 start-page: 436 year: 2019 end-page: 444 ident: bib0063 article-title: Disease duration and disability in dysfeRlinopathy can be described by muscle imaging using heatmaps and random forests publication-title: Muscle Nerve – volume: 22 start-page: S54 year: 2012 end-page: S67 ident: bib0051 article-title: Towards harmonization of protocols for mri outcome measures in skeletal muscle studies: consensus recommendations from two treat-nmd nmr workshops, 2 may 2010, stockholm, sweden, 1-2 october 2009, paris publication-title: France. Neuromuscul Disord. – volume: 34 start-page: 95 year: 2015 end-page: 108 ident: bib0024 article-title: Muscle mri in muscular dystrophies publication-title: Acta Myol – volume: 153 start-page: 189 year: 1984 end-page: 194 ident: bib0049 article-title: Simple proton spectroscopic imaging publication-title: Radiology – volume: 54 start-page: 192 year: 2016 end-page: 202 ident: bib0017 article-title: Pediatric laminopathies: whole-body magnetic resonance imaging fingerprint and comparison with sepn1 myopathy publication-title: Muscle Nerve – volume: 45 start-page: 273 year: 2014 end-page: 274 ident: bib0020 article-title: Muscle magnetic resonance imaging: a new diagnostic tool with promising avenues in therapeutic trials publication-title: Neuropediatrics – volume: 52 start-page: 512 year: 2015 end-page: 520 ident: bib0022 article-title: Whole-body magnetic resonance imaging evaluation of facioscapulohumeral muscular dystrophy publication-title: Muscle Nerve – volume: 3 start-page: 1 year: 2016 end-page: 28 ident: bib0073 article-title: Skeletal muscle quantitative nuclear magnetic resonance imaging and spectroscopy as an outcome measure for clinical trials publication-title: J Neuromuscul Dis – volume: 15 start-page: 65 year: 2016 end-page: 77 ident: bib0019 article-title: MRI biomarker assessment of neuromuscular disease progression: a prospective observational cohort study publication-title: Lancet Neurol – volume: 16 start-page: 731 year: 1998 end-page: 741 ident: bib0009 article-title: MRI in the study of distal primary myopathopies and of muscular alterations due to peripheral neuropathies: possible diagnostic capacities of mr equipment with low intensity field (0.2 T) dedicated to peripheral limbs publication-title: Magn Reson Imaging – volume: 54 start-page: 203 year: 2016 end-page: 210 ident: bib0018 article-title: Broadening the imaging phenotype of dysferlinopathy at different disease stages publication-title: Muscle Nerve – volume: 17 start-page: 517 year: 2007 end-page: 523 ident: bib0026 article-title: Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhood publication-title: Neuromuscul Disord – year: 2017 ident: bib0027 article-title: Myopathology in times of modern imaging publication-title: Neuropathol Appl Neurobiol – volume: 19 start-page: 530 year: 2007 end-page: 535 ident: bib0047 article-title: Skeletal muscle imaging and inflammatory myopathies publication-title: Curr Opin Rheumatol – volume: 23 start-page: 688 year: 2016 end-page: 703 ident: bib0015 article-title: Muscle imaging in inherited and acquired muscle diseases publication-title: Eur J Neurol – volume: 79 start-page: 1716 year: 2012 end-page: 1723 ident: bib0031 article-title: Reliability and accuracy of skeletal muscle imaging in limb-girdle muscular dystrophies publication-title: Neurology – volume: 5 year: 2016 ident: bib0046 article-title: Whole-body mri for full assessment and characterization of diffuse inflammatory myopathy publication-title: Acta Radiol Open – volume: 25 start-page: 5014 year: 2015 ident: bib0028 article-title: Role of radiologic imaging in genetic and acquired neuromuscular disorders publication-title: Eur J Transl Myol – volume: 52 start-page: 728 year: 2015 end-page: 735 ident: bib0072 article-title: Whole-body muscle magnetic resonance imaging in SEPN1-related myopathy shows a homogeneous and recognizable pattern publication-title: Muscle Nerve – volume: 13 start-page: 554 year: 2003 end-page: 558 ident: bib0043 article-title: Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and ullrich phenotype publication-title: Neuromuscul Disord – volume: 18 start-page: 526 year: 2005 end-page: 537 ident: bib0010 article-title: Muscle imaging in clinical practice: diagnostic value of muscle magnetic resonance imaging in inherited neuromuscular disorders publication-title: Curr Opin Neurol – volume: 22 start-page: 509 year: 2004 end-page: 538 ident: bib0011 article-title: MRI in myopathy publication-title: Neurol Clin – year: 2016 ident: bib0069 article-title: The sensitivity of exome sequencing in identifying pathogenic mutations for lgmd in the united states publication-title: J Hum Genet – volume: 22 start-page: S137 year: 2012 end-page: S147 ident: bib0016 article-title: Whole-Body muscle mri in a series of patients with congenital myopathy related to TPM2 gene mutations publication-title: Neuromuscul Disord – volume: 27 start-page: 78 year: 2017 end-page: 82 ident: bib0055 article-title: Tubular aggregate myopathy with features of stormorken disease due to a new STIM1 mutation publication-title: Neuromuscul Disord – year: 2016 ident: bib0034 article-title: Magnetic resonance imaging patterns of muscle involvement in genetic muscle diseases: a systematic review publication-title: J Neurol – volume: 3 start-page: 607 year: 2016 end-page: 622 ident: bib0065 article-title: Longitudinal mri quantification of muscle degeneration in duchenne muscular dystrophy publication-title: Ann Clin Transl Neurol – volume: 15 start-page: 303 year: 2005 end-page: 310 ident: bib0042 article-title: Muscle MRI in ullrich congenital muscular dystrophy and bethlem myopathy publication-title: Neuromuscul Disord – volume: 17 start-page: 67 year: 2015 ident: bib0048 article-title: Role of mri in diagnosis and management of idiopathic inflammatory myopathies publication-title: Curr Rheumatol Rep – volume: 51 start-page: 884 year: 2015 end-page: 889 ident: bib0061 article-title: Should patients with asymptomatic pompe disease be treated? a nationwide study in france publication-title: Muscle Nerve – volume: 26 start-page: 7 year: 2016 end-page: 15 ident: bib0068 article-title: Targeted next-generation sequencing assay for detection of mutations in primary myopathies publication-title: Neuromuscul Disord – volume: 6 start-page: 305 year: 2002 end-page: 307 ident: bib0003 article-title: A short protocol for muscle mri in children with muscular dystrophies publication-title: Eur J Paediatr Neurol – volume: 63 start-page: 946 year: 1990 end-page: 950 ident: bib0007 article-title: Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvement publication-title: Br J Radiol – volume: 95 start-page: 17 year: 2014 end-page: 26 ident: bib0045 article-title: Current and future imaging of the peripheral nervous system publication-title: Diagn Interv Imaging – volume: 120 start-page: 111 year: 2009 end-page: 118 ident: bib0071 article-title: Pattern of skeletal muscle involvement in primary dysferlinopathies: a whole-body 3.0-T magnetic resonance imaging study publication-title: Acta Neurol Scand – volume: 45 start-page: 605 year: 2018 end-page: 619 ident: bib0023 article-title: Neuromuscular ultrasound: Clinical applications and diagnostic values publication-title: Can J Neurol Sci – volume: 25 start-page: 433 year: 2007 end-page: 440 ident: bib0037 article-title: Muscle mri in inherited neuromuscular disorders: past, present, and future publication-title: J Magn Reson Imaging – volume: 18 start-page: 221 year: 2011 end-page: 229 ident: bib0032 article-title: Muscle imaging in congenital myopathies publication-title: Semin Pediatr Neurol – volume: 22 start-page: S122 year: 2012 end-page: S129 ident: bib0035 article-title: Muscle mri findings in limb girdle muscular dystrophy type 2L publication-title: Neuromuscul Disord – volume: 72 start-page: 1424 year: 2015 end-page: 1432 ident: bib0067 article-title: Use of whole-exome sequencing for diagnosis of limb-girdle muscular dystrophy: outcomes and lessons learned publication-title: JAMA Neurol – volume: 265 start-page: 2646 year: 2018 end-page: 2655 ident: bib0059 article-title: Quantitative muscle MRI and ultrasound for facioscapulohumeral muscular dystrophy: complementary imaging biomarkers publication-title: J Neurol – volume: 52 start-page: 334 year: 2015 end-page: 338 ident: bib0029 article-title: Muscle ultrasound quantifies disease progression over time in infants and young boys with duchenne muscular dystrophy publication-title: Muscle Nerve – volume: 22 start-page: S42 year: 2012 end-page: S53 ident: bib0002 article-title: TREAT-NMD workshop: pattern recognition in genetic muscle diseases using muscle MRI: 25-26 february 2011, rome, italy publication-title: Neuromuscul Disord. – year: 2019 ident: bib0057 article-title: HNRNPDL-related muscular dystrophy: expanding the clinical, morphological and mri phenotypes publication-title: J Neurol – volume: 430 start-page: 241 year: 2013 end-page: 244 ident: bib0062 article-title: Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene publication-title: Biochem Biophys Res Commun – volume: 8 start-page: 17 year: 2018 ident: bib0056 article-title: TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of alpha-dystroglycan and muscular dystrophy publication-title: Skelet Muscle – volume: 264 start-page: 438 year: 2017 end-page: 447 ident: bib0064 article-title: MRI as outcome measure in facioscapulohumeral muscular dystrophy: 1-year follow-up of 45 patients publication-title: J Neurol – volume: 264 start-page: 2053 year: 2017 end-page: 2067 ident: bib0074 article-title: Quantifying fat replacement of muscle by quantitative mri in muscular dystrophy publication-title: J Neurol – volume: 6 start-page: 1 year: 2019 end-page: 30 ident: bib0075 article-title: Exploration of new contrasts, targets, and mr imaging and spectroscopy techniques for neuromuscular disease - A Workshop report of working group 3 of the biomedicine and molecular biosciences cost action BM1304 myo-mri publication-title: J Neuromuscul Dis – volume: 22 start-page: S41 year: 2012 ident: bib0014 article-title: Applications of MRI in muscle diseases publication-title: Neuromuscul Disord – volume: 56 start-page: 1096 year: 2017 end-page: 1100 ident: bib0053 article-title: Hyperckemia and myalgia are common presentations of anoctamin-5-related myopathy in french patients publication-title: Muscle Nerve – volume: 22 start-page: 1483 year: 2013 end-page: 1492 ident: bib0044 article-title: The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis publication-title: Hum Mol Genet – volume: 43 start-page: 1113 year: 2014 end-page: 1122 ident: bib0054 article-title: Whole-body muscle mri to detect myopathies in non-extrapyramidal bent spine syndrome publication-title: Skeletal Radiol – volume: 37 start-page: 742 year: 2016 end-page: 748 ident: bib0041 article-title: Age- and Level-Dependence of fatty infiltration in lumbar paravertebral muscles of healthy volunteers publication-title: AJNR Am J Neuroradiol – volume: 9 start-page: 456 year: 2018 ident: bib0013 article-title: The diagnostic value of mri pattern recognition in distal myopathies publication-title: Front Neurol – volume: 26 start-page: 768 year: 2016 end-page: 774 ident: bib0066 article-title: Muscle mri in duchenne muscular dystrophy: Evidence of a distinctive pattern publication-title: Neuromuscul Disord – year: 2017 ident: 10.1016/j.nmd.2019.08.011_bib0021 article-title: Muscle mri in pediatrics: clinical, pathological and genetic correlation publication-title: Pediatr Radiol doi: 10.1007/s00247-016-3777-6 – volume: 45 start-page: 605 issue: 6 year: 2018 ident: 10.1016/j.nmd.2019.08.011_bib0023 article-title: Neuromuscular ultrasound: Clinical applications and diagnostic values publication-title: Can J Neurol Sci doi: 10.1017/cjn.2018.314 – volume: 28 start-page: 543 issue: 3 year: 2008 ident: 10.1016/j.nmd.2019.08.011_bib0050 article-title: Dixon techniques for water and fat imaging publication-title: J Magn Reson Imaging doi: 10.1002/jmri.21492 – volume: 72 start-page: 1424 issue: 12 year: 2015 ident: 10.1016/j.nmd.2019.08.011_bib0067 article-title: Use of whole-exome sequencing for diagnosis of limb-girdle muscular dystrophy: outcomes and lessons learned publication-title: JAMA Neurol doi: 10.1001/jamaneurol.2015.2274 – volume: 6 start-page: 309 issue: 6 year: 2002 ident: 10.1016/j.nmd.2019.08.011_bib0004 article-title: Muscle mri findings in a three-generation family affected by bethlem myopathy publication-title: Eur J Paediatr Neurol doi: 10.1053/ejpn.2002.0618 – volume: 59 start-page: 436 issue: 4 year: 2019 ident: 10.1016/j.nmd.2019.08.011_bib0063 article-title: Disease duration and disability in dysfeRlinopathy can be described by muscle imaging using heatmaps and random forests publication-title: Muscle Nerve doi: 10.1002/mus.26403 – volume: 264 start-page: 2053 issue: 10 year: 2017 ident: 10.1016/j.nmd.2019.08.011_bib0074 article-title: Quantifying fat replacement of muscle by quantitative mri in muscular dystrophy publication-title: J Neurol doi: 10.1007/s00415-017-8547-3 – volume: 18 start-page: 2922 issue: 12 year: 2008 ident: 10.1016/j.nmd.2019.08.011_bib0070 article-title: Involvement patterns in myotilinopathy and desminopathy detected by a novel neuromuscular whole-body mri protocol publication-title: Eur Radiol doi: 10.1007/s00330-008-1071-1 – volume: 27 start-page: 78 issue: 1 year: 2017 ident: 10.1016/j.nmd.2019.08.011_bib0055 article-title: Tubular aggregate myopathy with features of stormorken disease due to a new STIM1 mutation publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2016.10.006 – volume: 95 start-page: 17 issue: 1 year: 2014 ident: 10.1016/j.nmd.2019.08.011_bib0045 article-title: Current and future imaging of the peripheral nervous system publication-title: Diagn Interv Imaging doi: 10.1016/j.diii.2013.05.008 – volume: 209 start-page: 1340 issue: 6 year: 2017 ident: 10.1016/j.nmd.2019.08.011_bib0040 article-title: Sporadic inclusion body myositis: mri findings and correlation with clinical and functional parameters publication-title: AJR Am J Roentgenol doi: 10.2214/AJR.17.17849 – volume: 13 start-page: 554 issue: 7-8 year: 2003 ident: 10.1016/j.nmd.2019.08.011_bib0043 article-title: Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and ullrich phenotype publication-title: Neuromuscul Disord doi: 10.1016/S0960-8966(03)00091-9 – volume: 26 start-page: 33 issue: 1 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0039 article-title: Muscle imaging in muscle dystrophies produced by mutations in the emd and lmna genes publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2015.10.001 – volume: 34 start-page: 95 issue: 2-3 year: 2015 ident: 10.1016/j.nmd.2019.08.011_bib0024 article-title: Muscle mri in muscular dystrophies publication-title: Acta Myol – volume: 18 start-page: 221 issue: 4 year: 2011 ident: 10.1016/j.nmd.2019.08.011_bib0032 article-title: Muscle imaging in congenital myopathies publication-title: Semin Pediatr Neurol doi: 10.1016/j.spen.2011.10.003 – year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0034 article-title: Magnetic resonance imaging patterns of muscle involvement in genetic muscle diseases: a systematic review publication-title: J Neurol – volume: 264 start-page: 438 issue: 3 year: 2017 ident: 10.1016/j.nmd.2019.08.011_bib0064 article-title: MRI as outcome measure in facioscapulohumeral muscular dystrophy: 1-year follow-up of 45 patients publication-title: J Neurol doi: 10.1007/s00415-016-8361-3 – volume: 28 start-page: 5293 issue: 12 year: 2018 ident: 10.1016/j.nmd.2019.08.011_bib0058 article-title: Muscular MRI-based algorithm to differentiate inherited myopathies presenting with spinal rigidity publication-title: Eur Radiol doi: 10.1007/s00330-018-5472-5 – volume: 12 start-page: 631 issue: 7-8 year: 2002 ident: 10.1016/j.nmd.2019.08.011_bib0005 article-title: Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1) publication-title: Neuromuscul Disord doi: 10.1016/S0960-8966(02)00023-8 – volume: 15 start-page: 65 issue: 1 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0019 article-title: MRI biomarker assessment of neuromuscular disease progression: a prospective observational cohort study publication-title: Lancet Neurol doi: 10.1016/S1474-4422(15)00242-2 – volume: 21 start-page: 791 issue: 11 year: 2011 ident: 10.1016/j.nmd.2019.08.011_bib0033 article-title: Whole-body muscle mri in 20 patients suffering from late onset pompe disease: Involvement patterns publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2011.06.748 – volume: 5 issue: 9 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0046 article-title: Whole-body mri for full assessment and characterization of diffuse inflammatory myopathy publication-title: Acta Radiol Open – volume: 22 start-page: S42 issue: Suppl 2 year: 2012 ident: 10.1016/j.nmd.2019.08.011_bib0002 article-title: TREAT-NMD workshop: pattern recognition in genetic muscle diseases using muscle MRI: 25-26 february 2011, rome, italy publication-title: Neuromuscul Disord. doi: 10.1016/j.nmd.2012.08.002 – volume: 52 start-page: 728 issue: 5 year: 2015 ident: 10.1016/j.nmd.2019.08.011_bib0072 article-title: Whole-body muscle magnetic resonance imaging in SEPN1-related myopathy shows a homogeneous and recognizable pattern publication-title: Muscle Nerve doi: 10.1002/mus.24634 – volume: 22 start-page: S68 issue: Suppl 2 year: 2012 ident: 10.1016/j.nmd.2019.08.011_bib0001 article-title: Whole body muscle mri protocol: pattern recognition in early onset nm disorders publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2012.08.003 – volume: 22 start-page: S41 issue: Suppl 2 year: 2012 ident: 10.1016/j.nmd.2019.08.011_bib0014 article-title: Applications of MRI in muscle diseases publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2012.08.001 – volume: 62 start-page: 326 issue: 736 year: 1989 ident: 10.1016/j.nmd.2019.08.011_bib0008 article-title: Acute rhabdomyolysis: evaluation with magnetic resonance imaging compared with computed tomography and ultrasonography publication-title: Br J Radiol doi: 10.1259/0007-1285-62-736-326 – volume: 8 start-page: 17 issue: 1 year: 2018 ident: 10.1016/j.nmd.2019.08.011_bib0056 article-title: TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of alpha-dystroglycan and muscular dystrophy publication-title: Skelet Muscle doi: 10.1186/s13395-018-0163-0 – volume: 16 start-page: 731 issue: 7 year: 1998 ident: 10.1016/j.nmd.2019.08.011_bib0009 article-title: MRI in the study of distal primary myopathopies and of muscular alterations due to peripheral neuropathies: possible diagnostic capacities of mr equipment with low intensity field (0.2 T) dedicated to peripheral limbs publication-title: Magn Reson Imaging doi: 10.1016/S0730-725X(98)00080-0 – volume: 22 start-page: S122 issue: Suppl 2 year: 2012 ident: 10.1016/j.nmd.2019.08.011_bib0035 article-title: Muscle mri findings in limb girdle muscular dystrophy type 2L publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2012.05.012 – volume: 153 start-page: 189 issue: 1 year: 1984 ident: 10.1016/j.nmd.2019.08.011_bib0049 article-title: Simple proton spectroscopic imaging publication-title: Radiology doi: 10.1148/radiology.153.1.6089263 – volume: 63 start-page: 946 issue: 756 year: 1990 ident: 10.1016/j.nmd.2019.08.011_bib0007 article-title: Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvement publication-title: Br J Radiol doi: 10.1259/0007-1285-63-756-946 – volume: 19 start-page: 530 issue: 6 year: 2007 ident: 10.1016/j.nmd.2019.08.011_bib0047 article-title: Skeletal muscle imaging and inflammatory myopathies publication-title: Curr Opin Rheumatol doi: 10.1097/BOR.0b013e3282efdc66 – volume: 22 start-page: S137 issue: Suppl 2 year: 2012 ident: 10.1016/j.nmd.2019.08.011_bib0016 article-title: Whole-Body muscle mri in a series of patients with congenital myopathy related to TPM2 gene mutations publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2012.06.347 – volume: 430 start-page: 241 issue: 1 year: 2013 ident: 10.1016/j.nmd.2019.08.011_bib0062 article-title: Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene publication-title: Biochem Biophys Res Commun doi: 10.1016/j.bbrc.2012.10.127 – volume: 6 start-page: 305 issue: 6 year: 2002 ident: 10.1016/j.nmd.2019.08.011_bib0003 article-title: A short protocol for muscle mri in children with muscular dystrophies publication-title: Eur J Paediatr Neurol doi: 10.1053/ejpn.2002.0617 – volume: 23 start-page: 688 issue: 4 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0015 article-title: Muscle imaging in inherited and acquired muscle diseases publication-title: Eur J Neurol doi: 10.1111/ene.12984 – volume: 20 start-page: 2447 issue: 10 year: 2010 ident: 10.1016/j.nmd.2019.08.011_bib0052 article-title: Neuromuscular imaging in inherited muscle diseases publication-title: Eur Radiol doi: 10.1007/s00330-010-1799-2 – year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0069 article-title: The sensitivity of exome sequencing in identifying pathogenic mutations for lgmd in the united states publication-title: J Hum Genet – volume: 265 start-page: 2646 issue: 11 year: 2018 ident: 10.1016/j.nmd.2019.08.011_bib0059 article-title: Quantitative muscle MRI and ultrasound for facioscapulohumeral muscular dystrophy: complementary imaging biomarkers publication-title: J Neurol doi: 10.1007/s00415-018-9037-y – volume: 3 start-page: 607 issue: 8 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0065 article-title: Longitudinal mri quantification of muscle degeneration in duchenne muscular dystrophy publication-title: Ann Clin Transl Neurol doi: 10.1002/acn3.319 – volume: 15 start-page: 230 issue: 3 year: 1992 ident: 10.1016/j.nmd.2019.08.011_bib0006 article-title: Imaging techniques in myotonic dystrophy. a comparative study of ultrasound, computed tomography and magnetic resonance imaging of skeletal muscles publication-title: Eur J Radiol doi: 10.1016/0720-048X(92)90113-N – volume: 37 start-page: 742 issue: 4 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0041 article-title: Age- and Level-Dependence of fatty infiltration in lumbar paravertebral muscles of healthy volunteers publication-title: AJNR Am J Neuroradiol doi: 10.3174/ajnr.A4596 – volume: 22 start-page: 509 issue: 3 year: 2004 ident: 10.1016/j.nmd.2019.08.011_bib0011 article-title: MRI in myopathy publication-title: Neurol Clin doi: 10.1016/j.ncl.2004.03.008 – volume: 79 start-page: 1716 issue: 16 year: 2012 ident: 10.1016/j.nmd.2019.08.011_bib0031 article-title: Reliability and accuracy of skeletal muscle imaging in limb-girdle muscular dystrophies publication-title: Neurology doi: 10.1212/WNL.0b013e31826e9b73 – volume: 29 start-page: 614 issue: 5 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0030 article-title: Recent developments in muscle imaging of neuromuscular disorders publication-title: Curr Opin Neurol doi: 10.1097/WCO.0000000000000364 – volume: 25 start-page: 5014 issue: 2 year: 2015 ident: 10.1016/j.nmd.2019.08.011_bib0028 article-title: Role of radiologic imaging in genetic and acquired neuromuscular disorders publication-title: Eur J Transl Myol doi: 10.4081/bam.2015.2.121 – volume: 22 start-page: S54 issue: Suppl 2 year: 2012 ident: 10.1016/j.nmd.2019.08.011_bib0051 article-title: Towards harmonization of protocols for mri outcome measures in skeletal muscle studies: consensus recommendations from two treat-nmd nmr workshops, 2 may 2010, stockholm, sweden, 1-2 october 2009, paris publication-title: France. Neuromuscul Disord. doi: 10.1016/j.nmd.2012.06.005 – volume: 54 start-page: 203 issue: 2 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0018 article-title: Broadening the imaging phenotype of dysferlinopathy at different disease stages publication-title: Muscle Nerve doi: 10.1002/mus.25045 – volume: 45 start-page: 273 issue: 5 year: 2014 ident: 10.1016/j.nmd.2019.08.011_bib0020 article-title: Muscle magnetic resonance imaging: a new diagnostic tool with promising avenues in therapeutic trials publication-title: Neuropediatrics doi: 10.1055/s-0034-1389894 – volume: 15 start-page: 303 issue: 4 year: 2005 ident: 10.1016/j.nmd.2019.08.011_bib0042 article-title: Muscle MRI in ullrich congenital muscular dystrophy and bethlem myopathy publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2005.01.004 – volume: 9 start-page: 456 year: 2018 ident: 10.1016/j.nmd.2019.08.011_bib0013 article-title: The diagnostic value of mri pattern recognition in distal myopathies publication-title: Front Neurol doi: 10.3389/fneur.2018.00456 – volume: 56 start-page: 1096 issue: 6 year: 2017 ident: 10.1016/j.nmd.2019.08.011_bib0053 article-title: Hyperckemia and myalgia are common presentations of anoctamin-5-related myopathy in french patients publication-title: Muscle Nerve doi: 10.1002/mus.25608 – volume: 51 start-page: 884 issue: 6 year: 2015 ident: 10.1016/j.nmd.2019.08.011_bib0061 article-title: Should patients with asymptomatic pompe disease be treated? a nationwide study in france publication-title: Muscle Nerve doi: 10.1002/mus.24653 – volume: 26 start-page: 768 issue: 11 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0066 article-title: Muscle mri in duchenne muscular dystrophy: Evidence of a distinctive pattern publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2016.09.002 – volume: 67 start-page: 201 issue: 2 year: 2010 ident: 10.1016/j.nmd.2019.08.011_bib0012 article-title: Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine publication-title: Ann Neurol doi: 10.1002/ana.21846 – volume: 3 start-page: 1 issue: 1 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0073 article-title: Skeletal muscle quantitative nuclear magnetic resonance imaging and spectroscopy as an outcome measure for clinical trials publication-title: J Neuromuscul Dis doi: 10.3233/JND-160145 – volume: 18 start-page: 526 issue: 5 year: 2005 ident: 10.1016/j.nmd.2019.08.011_bib0010 article-title: Muscle imaging in clinical practice: diagnostic value of muscle magnetic resonance imaging in inherited neuromuscular disorders publication-title: Curr Opin Neurol doi: 10.1097/01.wco.0000183947.01362.fe – volume: 33 start-page: 1 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0025 article-title: Skeletal muscle imaging in neuromuscular disease publication-title: J Clin Neurosci doi: 10.1016/j.jocn.2016.01.041 – year: 2017 ident: 10.1016/j.nmd.2019.08.011_bib0027 article-title: Myopathology in times of modern imaging publication-title: Neuropathol Appl Neurobiol doi: 10.1111/nan.12385 – volume: 17 start-page: 517 issue: 7 year: 2007 ident: 10.1016/j.nmd.2019.08.011_bib0026 article-title: Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhood publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2007.03.015 – start-page: 78 issue: 304 year: 1994 ident: 10.1016/j.nmd.2019.08.011_bib0036 article-title: Fatty muscle degeneration in cuff ruptures. Pre- and postoperative evaluation by CT scan publication-title: Clin Orthop Relat Res. – volume: 14 start-page: 1489 issue: 8 year: 2004 ident: 10.1016/j.nmd.2019.08.011_bib0038 article-title: Whole-body mr screening of muscles in the evaluation of neuromuscular diseases publication-title: Eur Radiol doi: 10.1007/s00330-004-2270-z – volume: 12 issue: 7 year: 2017 ident: 10.1016/j.nmd.2019.08.011_bib0060 article-title: An efficacy analysis of whole-body magnetic resonance imaging in the diagnosis and follow-up of polymyositis and dermatomyositis publication-title: PLoS One doi: 10.1371/journal.pone.0181069 – volume: 6 start-page: 1 issue: 1 year: 2019 ident: 10.1016/j.nmd.2019.08.011_bib0075 article-title: Exploration of new contrasts, targets, and mr imaging and spectroscopy techniques for neuromuscular disease - A Workshop report of working group 3 of the biomedicine and molecular biosciences cost action BM1304 myo-mri publication-title: J Neuromuscul Dis doi: 10.3233/JND-180333 – volume: 52 start-page: 334 issue: 3 year: 2015 ident: 10.1016/j.nmd.2019.08.011_bib0029 article-title: Muscle ultrasound quantifies disease progression over time in infants and young boys with duchenne muscular dystrophy publication-title: Muscle Nerve doi: 10.1002/mus.24609 – volume: 120 start-page: 111 issue: 2 year: 2009 ident: 10.1016/j.nmd.2019.08.011_bib0071 article-title: Pattern of skeletal muscle involvement in primary dysferlinopathies: a whole-body 3.0-T magnetic resonance imaging study publication-title: Acta Neurol Scand doi: 10.1111/j.1600-0404.2008.01129.x – volume: 17 start-page: 67 issue: 11 year: 2015 ident: 10.1016/j.nmd.2019.08.011_bib0048 article-title: Role of mri in diagnosis and management of idiopathic inflammatory myopathies publication-title: Curr Rheumatol Rep doi: 10.1007/s11926-015-0544-x – volume: 43 start-page: 1113 issue: 8 year: 2014 ident: 10.1016/j.nmd.2019.08.011_bib0054 article-title: Whole-body muscle mri to detect myopathies in non-extrapyramidal bent spine syndrome publication-title: Skeletal Radiol doi: 10.1007/s00256-014-1909-3 – year: 2019 ident: 10.1016/j.nmd.2019.08.011_bib0057 article-title: HNRNPDL-related muscular dystrophy: expanding the clinical, morphological and mri phenotypes publication-title: J Neurol doi: 10.1007/s00415-019-09437-3 – volume: 25 start-page: 433 issue: 2 year: 2007 ident: 10.1016/j.nmd.2019.08.011_bib0037 article-title: Muscle mri in inherited neuromuscular disorders: past, present, and future publication-title: J Magn Reson Imaging doi: 10.1002/jmri.20804 – volume: 52 start-page: 512 issue: 4 year: 2015 ident: 10.1016/j.nmd.2019.08.011_bib0022 article-title: Whole-body magnetic resonance imaging evaluation of facioscapulohumeral muscular dystrophy publication-title: Muscle Nerve doi: 10.1002/mus.24569 – volume: 54 start-page: 192 issue: 2 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0017 article-title: Pediatric laminopathies: whole-body magnetic resonance imaging fingerprint and comparison with sepn1 myopathy publication-title: Muscle Nerve doi: 10.1002/mus.25018 – volume: 22 start-page: 1483 issue: 8 year: 2013 ident: 10.1016/j.nmd.2019.08.011_bib0044 article-title: The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis publication-title: Hum Mol Genet doi: 10.1093/hmg/dds514 – volume: 26 start-page: 7 issue: 1 year: 2016 ident: 10.1016/j.nmd.2019.08.011_bib0068 article-title: Targeted next-generation sequencing assay for detection of mutations in primary myopathies publication-title: Neuromuscul Disord doi: 10.1016/j.nmd.2015.10.003 |
SSID | ssj0015767 |
Score | 2.491504 |
SecondaryResourceType | review_article |
Snippet | •Whole body MRI (WBMRI) is an important imaging biomarker for myopathies.•Different mutations within the same gene can have different clinical WBMRI... Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and characterizing the progression of myopathies and muscular... |
SourceID | hal proquest pubmed crossref elsevier |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 827 |
SubjectTerms | Congenital myopathy Humans Inflammatory myopathy Inherited myopathy Life Sciences Limb girdle muscular dystrophy Magnetic resonance imaging Magnetic Resonance Imaging - methods Muscular Diseases - diagnostic imaging Muscular Diseases - genetics Whole Body Imaging - methods Whole-body MRI |
Title | MYO-MRI diagnostic protocols in genetic myopathies |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S0960896619311022 https://dx.doi.org/10.1016/j.nmd.2019.08.011 https://www.ncbi.nlm.nih.gov/pubmed/31727541 https://www.proquest.com/docview/2315102420 https://hal.science/hal-03488911 |
Volume | 29 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LS8NAEB5sBfEivq0vongSYrO72WRzLEWpjyr4AD0t2WSLFU3FtoIXf7szeYEHFTxmmQnLzOzsN-w8AA5swGzkc-bakA0wQAl9N-YiQIXELDKWGRNT7XD_Mujd-Wf38n4GulUtDKVVlr6_8Om5ty5X2qU026_DYfuGwLdCtI4QhFHc0oBZjre9asJs5_S8d1k_JiCkzqumkd4lhupxM0_zyl6oXyiL8kaejP10PTUeKU_yJxCaX0Yni7BQokinU2x0CWZstgxz_fKdfAV4_-HK7V-fOmmRSYdkDnVkGKHax84wc9BsqHrRefkY5TOJ7XgV7k6Ob7s9t5yO4Ca-CCeu9IxI0khGMg1EHAnfpNQJxoSeCeQgoALSVDKVWCXiGAMXqXiCBzDkxqjUG4RiDZrZKLMb4EQcgYi1SiqDkTIqSGGcwRG7SMFNEqkWeJVQdFK2DqcJFs-6yhF70ihHTXLUNNWSsRYc1iyvRd-M34h5JWldFYSiC9Po1X9j8mumbxbzF9s-qrLeE3XX7nUuNK15Ar0ZOv93JNqrNK3xuNEbSpzZ0XSsEQ6jEBHXeC1YL0yg_pcgMCh9tvm_nW3BPH0VhY7b0Jy8Te0OIp6J2YXG0SfbLe36C8-Z-Tc |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3da9swED_aFLq-lH5tTT9Wd-ypYGJJli0_htLiNHEKWwrdk7BshWWsTmnSwv773fkL9pAU9irfGXF3Ov0O3QfAVxswG_mcuTZkUwxQQt9NuQhQISmLjGXGpFQ7nIyD-MG_e5SPG3Dd1MJQWmXt-yufXnrreqVXS7P3PJv1vhP4VojWEYIwils2YcunodYd2OoPhvG4fUxASF1WTSO9SwzN42aZ5lU8Ub9QFpWNPBlbdT1t_qQ8yVUgtLyMbvdgt0aRTr_a6D5s2OIAtpP6nfwQePLj3k2-DZy8yqRDMoc6MsxR7QtnVjhoNlS96Dz9mZczie3iCB5ubybXsVtPR3AzX4RLV3pGZHkkI5kHIo2Eb3LqBGNCzwRyGlABaS6ZyqwSaYqBi1Q8wwMYcmNU7k1D8RE6xbywx-BEHIGItUoqg5EyKkhhnMERu0jBTRapLniNUHRWtw6nCRa_dZMj9kujHDXJUdNUS8a6cNWyPFd9M9YR80bSuikIRRem0auvY_Jbpn8s5j22L6jKdk_UXTvujzSteQK9GTr_NyS6bDSt8bjRG0pa2PnrQiMcRiEirvG68KkygfZfgsAgWuDJ_-3sAj7Ek2SkR4Px8BR26EtV9HgGneXLqz1H9LM0n2vr_guutfsd |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=MYO-MRI+diagnostic+protocols+in+genetic+myopathies&rft.jtitle=Neuromuscular+disorders+%3A+NMD&rft.au=Warman+Chardon%2C+Jodi&rft.au=D%C3%ADaz-Manera%2C+Jordi&rft.au=Tasca%2C+Giorgio&rft.au=B%C3%B6nnemann%2C+Carsten+G&rft.date=2019-11-01&rft.eissn=1873-2364&rft.volume=29&rft.issue=11&rft.spage=827&rft_id=info:doi/10.1016%2Fj.nmd.2019.08.011&rft_id=info%3Apmid%2F31727541&rft.externalDocID=31727541 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0960-8966&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0960-8966&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0960-8966&client=summon |